Allele Registry

Canonical Allele Identifier: PA2826262532

Gene: CUX1 HGNC NCBI

ClinVar RCV:

RCV000880414

RCV003940410

ClinVar Variation:

709065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001189472.1:p.Val99Ile	CA4410396 NM_001202543.2:c.295G>A